Canonical Allele Identifier: CA2639799
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs769492668
ExAC: 3:138665397 C / T
gnomAD v2: 3-138665397-C-T
gnomAD v4: 3-138946555-C-T
COSMIC: COSM23415
MyVariant Identifiers: chr3:g.138665397C>T (hg19) chr3:g.138946555C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946555C>T , CM000665.2:g.138946555C>T GRCh38
NC_000003.11:g.138665397C>T , CM000665.1:g.138665397C>T GRCh37
NC_000003.10:g.140148087C>T NCBI36
NG_012454.1:g.5586G>A
NG_029796.1:g.4322C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.168G>A MANE Select ENSP00000497217.1:p.Pro56=
ENST00000330315.3:c.168G>A ENSP00000333188.3:p.Pro56=
NM_023067.3:c.168G>A NP_075555.1:p.Pro56=
NM_023067.4:c.168G>A MANE Select NP_075555.1:p.Pro56=
Search 100 bp 5'
Search 100 bp 3'